Oxidative rearrangement of 3-aryl-1H-benzo[f]chromenes into 2-aroyl-1,2-dihydronaphtho[2,1-b]furans View Full Text


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Article Info

DATE

2021-05

AUTHORS

Kirill S. Korzhenko, Dmitry V. Osipov, Vitaly А. Osyanin, Maxim R. Demidov, Yuri N. Klimochkin

ABSTRACT

By the reaction of 3-aryl-1H-benzo[f]chromenes with N-bromosuccinimide in aqueous acetone, a series of 2-aroyl-1,2-dihydronaphtho-[2,1-b]furans unsubstituted at the C-1 position were obtained as a result of formal addition of hypobromous acid to the pyran fragment and intramolecular nucleophilic substitution. This reaction is a rare example of the ring constriction in 1H-benzo[f]chromene series. More... »

PAGES

599-601

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10593-021-02949-9

DOI

http://dx.doi.org/10.1007/s10593-021-02949-9

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1138609147


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